A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268378



Internal ID20835418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42801826..42802718hg38UCSC Ensembl
chr5:42801928..42802820hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557405
Supporting Variants
Samples
Known GenesCCDC152, SEPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268378
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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